Overview

Being one of the prosperous countries in South America, Chile attracts medicinal products and medical device manufacturers to invest in the region not only for its strong healthcare system, but also for modern technologies that are being implemented. To access the market, manufacturers must obtain market approvals and registrations from the Agencia Nacional de Medicamentos (ANAMED). With ever-evolving Regulations and competitive timelines, Chilean market, however, challenges foreign manufacturers to navigate the updated Regulatory procedures to fall in compliance.

As a proven global Regulatory partner, Freyr assists foreign manufacturers with proficient Regulatory affairs consulting: right from decoding necessary regulations to preparing audit-ready dossiers and submitting them to concerned authorities for in-time market approvals. Freyr’s Regulatory services in Chile span across:

  • Medical Devices
  • Drugs
  • Food Supplements

Freyr Capabilities

  • Strategic Regulatory Consulting
  • Regulatory Affairs & Regulatory intelligence
  • Registration pathways and license management services
  • Dossier Management

Freyr Advantages

  • Strategic and well-versed local regulatory knowledgebase – with medical device, Regulatory health authority
  • Regulatory team with proven global RA expertise
  • Proactive and Collaborative approach
  • Quick turnarounds and faster time-to-market
  • Keeping abreast with region-specific legislation and Regulatory guidelines